| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 10151 | BAA01g08280 | A01 | 3625803 | G | A | upstream_gene_variant | MODIFIER | c.-360C>T| |
S34 |
| 10152 | BAA01g08290 | A01 | 3627413 | C | T | missense_variant | MODERATE | c.883G>A|p.Ala295Thr |
S185 |
| 10153 | BAA01g08290 | A01 | 3628433 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.214-1G>A| |
S305 |
| 10154 | BAA01g08280 | A01 | 3628552 | G | A | upstream_gene_variant | MODIFIER | c.-3109C>T| |
S97 |
| 10155 | BAA01g08280 | A01 | 3629190 | C | T | upstream_gene_variant | MODIFIER | c.-3747G>A| |
S103 |
| 10156 | BAA01g08280 | A01 | 3630323 | G | A | upstream_gene_variant | MODIFIER | c.-4880C>T| |
S9 |
| 10157 | BAA01g08290 | A01 | 3631862 | G | A | upstream_gene_variant | MODIFIER | c.-2977C>T| |
S197 |
| 10158 | BAA01g08290 | A01 | 3632724 | G | A | upstream_gene_variant | MODIFIER | c.-3839C>T| |
S23 |
| 10159 | BAA01g08290 | A01 | 3632859 | G | A | upstream_gene_variant | MODIFIER | c.-3974C>T| |
S162 |
| 10160 | BAA01g08290 | A01 | 3633401 | C | T | upstream_gene_variant | MODIFIER | c.-4516G>A| |
S1 S228 S289 S290 S90 |
| 10161 | BAA01g08300 | A01 | 3635052 | C | T | upstream_gene_variant | MODIFIER | c.-1737G>A| |
S61 |
| 10162 | BAA01g08300 | A01 | 3635108 | C | G | upstream_gene_variant | MODIFIER | c.-1793G>C| |
S65 |
| 10163 | BAA01g08300 | A01 | 3635135 | C | T | upstream_gene_variant | MODIFIER | c.-1820G>A| |
S36 |
| 10164 | BAA01g08300 | A01 | 3635779 | G | A | upstream_gene_variant | MODIFIER | c.-2464C>T| |
S38 |
| 10165 | BAA01g08300 | A01 | 3635797 | C | T | upstream_gene_variant | MODIFIER | c.-2482G>A| |
S155 S211 |
| 10166 | BAA01g08310 | A01 | 3636414 | G | A | synonymous_variant | LOW | c.2676C>T|p.Ser892Ser |
S124 |
| 10167 | BAA01g08310 | A01 | 3636435 | C | T | synonymous_variant | LOW | c.2655G>A|p.Glu885Glu |
S270 |
| 10168 | BAA01g08300 | A01 | 3636567 | G | A | upstream_gene_variant | MODIFIER | c.-3252C>T| |
S69 |
| 10169 | BAA01g08310 | A01 | 3637049 | C | T | missense_variant | MODERATE | c.2222G>A|p.Gly741Asp |
S179 S63 |
| 10170 | BAA01g08300 | A01 | 3637616 | G | A | upstream_gene_variant | MODIFIER | c.-4301C>T| |
S301 S304 |
| 10171 | BAA01g08310 | A01 | 3638638 | G | A | synonymous_variant | LOW | c.1416C>T|p.Arg472Arg |
S281 |
| 10172 | BAA01g08320 | A01 | 3640465 | G | A | downstream_gene_variant | MODIFIER | c.*4457C>T| |
S32 |
| 10173 | BAA01g08310 | A01 | 3640724 | G | A | missense_variant | MODERATE | c.92C>T|p.Pro31Leu |
S13 |
| 10174 | BAA01g08320 | A01 | 3640776 | G | A | downstream_gene_variant | MODIFIER | c.*4146C>T| |
S259 |
| 10175 | BAA01g08310 | A01 | 3640910 | G | A | missense_variant | MODERATE | c.11C>T|p.Ser4Phe |
S116 |